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논문 기본 정보

자료유형
학술저널
저자정보
Yang Yu (Southwest Medical University) Yan Deng (Department of Histology and Embryology School of Basic Medical Sciences Southwest Medical University) Yang Yu (Southwest Medical University) Wei Dong (Southwest Medical University (China)) Yi Han (Department of Histology and Embryology School of Basic Medical Sciences Southwest Medical University) Sheng Gao (Southwest Medical University (China))
저널정보
대한내분비학회 Endocrinology and Metabolism Endocrinology and Metabolism Vol.38 No.2
발행연도
2023.4
수록면
190 - 202 (13page)
DOI
https://doi.org/10.3803/EnM.2022.1599

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Type II deiodinase (DIO2) is thought to provide triiodothyronine (T3) to the nucleus to meet intracellular needs by deiodinating theprohormone thyroxine. DIO2 is expressed widely in many tissues and plays an important role in a variety of physiological processes,such as controlling T3 content in developing tissues (e.g., bone, muscles, and skin) and the adult brain, and regulating adaptive thermogenesis in brown adipose tissue (BAT). However, the identification and cloning of DIO2 have been challenging. In recent years,several clinical investigations have focused on the Thr92Ala polymorphism, which is closely correlated with clinical syndromessuch as type 2 diabetes, obesity, hypertension, and osteoarthritis. Thr92Ala-DIO2 was also found to be related to bone and neurodegenerative diseases and tumors. However, relatively few reviews have synthesized research on individual deiodinases, especiallyDIO2, in the past 5 years. This review summarizes current knowledge regarding the physiological functions of DIO2 in thyroid hormone signaling and adaptive thermogenesis in BAT and the brain, as well as the associations between Thr92Ala-DIO2 and bone andneurodegenerative diseases and tumors. This discussion is expected to provide insights into the physiological functions of DIO2 andthe clinical syndromes associated with Thr92Ala-DIO2.

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